美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
71610-192-60	71610-192	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	Zolpidem Tartrate	TABLET, FILM COATED	ORAL	20181108	N/A	ANDA	ANDA078413	Aphena Pharma Solutions - Tennessee, LLC	ZOLPIDEM TARTRATE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71610-192-60)
70518-3943-0	70518-3943	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	Zolpidem Tartrate	TABLET, FILM COATED	ORAL	20231208	N/A	ANDA	ANDA078413	REMEDYREPACK INC.	ZOLPIDEM TARTRATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3943-0)
70518-3943-1	70518-3943	HUMAN PRESCRIPTION DRUG	Zolpidem Tartrate	Zolpidem Tartrate	TABLET, FILM COATED	ORAL	20260608	N/A	ANDA	ANDA078413	REMEDYREPACK INC.	ZOLPIDEM TARTRATE	10 mg/1	100 POUCH in 1 BOX (70518-3943-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-3943-2)